Hane Masaya, Matsuoka Shuhei, Ono Sayaka, Miyata Shinji, Kitajima Ken, Sato Chihiro
Bioscience and Biotechnology Center School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.
Bioscience and Biotechnology Center.
Glycobiology. 2015 Oct;25(10):1112-24. doi: 10.1093/glycob/cwv049. Epub 2015 Jul 11.
Polysialic acid (polySia) is a linear polymer of sialic acid that modifies neural cell adhesion molecule (NCAM) in the vertebrate brain. PolySia is a large and exclusive molecule that functions as a negative regulator of cell-cell interactions. Recently, we demonstrated that polySia can specifically bind fibroblast growth factor 2 (FGF2) and BDNF; however, the protective effects of polySia on the proteolytic cleavage of these proteins remain unknown, although heparin/heparan sulfate has been shown to impair the cleavage of FGF2 by trypsin. Here, we analyzed the protective effects of polySia on the proteolytic cleavage of FGF2 and proBDNF/BDNF. We found that polySia protected intact FGF2 from tryptic activity via the specific binding of extended polySia chains on NCAM to FGF2. Oligo/polySia also functioned to impair the processing of proBDNF by plasmin via binding of oligo/polySia chains on NCAM. In addition, the polySia structure synthesized by mutated polysialyltransferase, ST8SIA2/STX(SNP7), which was previously identified from a schizophrenia patient, was impaired for these functions compared with polySia produced by normal ST8SIA2. Taken together, these data suggest that the protective effects of polySia toward FGF2 and proBDNF may be involved in the regulation of the concentrations of these neurologically active molecules.
多唾液酸(polySia)是唾液酸的线性聚合物,可修饰脊椎动物大脑中的神经细胞黏附分子(NCAM)。PolySia是一种大型且独特的分子,作为细胞间相互作用的负调节因子发挥作用。最近,我们证明了polySia可以特异性结合成纤维细胞生长因子2(FGF2)和脑源性神经营养因子(BDNF);然而,尽管肝素/硫酸乙酰肝素已被证明会损害胰蛋白酶对FGF2的切割,但polySia对这些蛋白质蛋白水解切割的保护作用仍然未知。在这里,我们分析了polySia对FGF2和前体BDNF/BDNF蛋白水解切割的保护作用。我们发现,polySia通过NCAM上延伸的polySia链与FGF2的特异性结合,保护完整的FGF2免受胰蛋白酶活性的影响。寡聚/多唾液酸还通过NCAM上的寡聚/多唾液酸链结合,发挥作用损害纤溶酶对前体BDNF的加工。此外,与正常ST8SIA2产生的polySia相比,由先前从一名精神分裂症患者中鉴定出的突变多唾液酸转移酶ST8SIA2/STX(SNP7)合成的polySia结构在这些功能上受损。综上所述,这些数据表明,polySia对FGF2和前体BDNF的保护作用可能参与了这些神经活性分子浓度的调节。